[PDF] Top 20 Case Report: Cystinuria and Polycystic Kidney Disease
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Case Report: Cystinuria and Polycystic Kidney Disease
... Patient A is now a 16-year-old male from Honduras with a 6-year history of nephrolithiasis who originally presented to our institution acutely in September 2012 with a symptomatic 2-mm left ureterovesical junction ... See full document
5
Autosomal dominant polycystic kidney disease and minimal trauma: medical review and case report
... the kidney (Table 2) ...gle kidney, did not respond optimally to hemodynamic sup- port (2 transfusions and fluid resuscitation) and given the availability of an expert interventional radiology team, the ... See full document
7
www.ijcep.com /IJCEP706003 Case Report Adult Polycystic Kidney Disease: A Disorder of Connective Tissue?
... a case of Caroli’s syndrome a few years back in our ...the disease process both in ADPKD and in liver of Caroli’s ...having polycystic kidney disease and APCKD patients having hepatic ... See full document
7
Management of delivery of a fetus with autosomal recessive polycystic kidney disease: a case report of abdominal dystocia and review of the literature
... renal polycystic kidney disease (ARPKD) is a rare form of cystic kidney disease, occur- ring in approximately 1 in 20,000 live births ...(polycystic kidney and hepatic ... See full document
5
Thyroid-like follicular carcinoma of the kidney in a patient with nephrolithiasis and polycystic kidney disease: a case report
... the kidney (TLFC), a rare neoplasm with low malignant potential, is histologically similar to primary thyroid follicular carcinoma, but characteristically lacks thyroid immunohistochemical ...We report a ... See full document
6
Autosomal dominant polycystic kidney disease with diffuse proliferative glomerulonephritis an unusual association: a case report and review of the literature
... change disease, crescentic glomerulonephritis, immunoglobulin A (IgA) nephropathy, mesangioprolifer- ative glomerulonephritis, diabetic glomerulosclerosis and ... See full document
5
Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease – a case report
... dominant polycystic kidney disease (ADPKD; OMIM *601313 for PKD1, and *173910 for PKD2) is the most common hereditary kidney disease, predominantly characterized by the presence of ... See full document
7
Incidental renal cell carcinoma presenting in a renal transplant recipient with autosomal dominant polycystic kidney disease: a case report
... The final pathological diagnosis was a type 2 papil- lary RCC, eosinophilic variant, pT1a (Figure 2C,D). The quadruple immunosuppression induction protocol comprised cyclosporine, mycophenolate mofetil, basi- liximab and ... See full document
5
The Association between Autosomal Dominant Polycystic Kidney Disease and Renal Cell Carcinoma
... 2013 Bilateral Papillary Renal Cell Carcinoma and Angiomyolipoma in the Patients with Autosomal Dominant Polycystic Kidney Disease: Case Report of Two Cases and Literature Review.. 2012 [r] ... See full document
7
Hyperuricemia and deterioration of renal function in autosomal dominant polycystic kidney disease
... Several mechanisms were proposed to explain renal dysfunction by hyperuricemia. First, association be- tween increased sUA level and cardiovascular disease has been reported [20]. In our study, no difference in ... See full document
8
Simultaneous occurrence of renal cell carcinoma and angiomyolipoma in the same kidney
... Conventional type RCC is the most common and poorly understood tumor in both clinical and pathological aspects. Hereditary factors may play an important role in development of RCC and also RCC can be associated with ... See full document
6
Successful pre-emptive kidney transplantation in a cystinuria patient with nephrolithiasis-related end-stage renal disease
... for cystinuria, renal replacement may poten- tially be useful in patients who have rare hereditary forms of kidney stone diseases, including ...this case will be helpful to others facing the problem ... See full document
5
Imaging of kidney cysts and cystic kidney diseases in children: an international working group consensus statement
... focal disease (simple and complex kidney cysts), afect a whole kidney (eg, multicystic dysplastic kid- ney or cystic dysplasia), or manifest as bilateral cystic disease (eg, autosomal ... See full document
15
Autosomal Recessive Polycystic Kidney Disease: A Hepatorenal Fibrocystic Disorder With Pleiotropic Effects
... of disease mechanisms into effec- tive ...track disease response is predicated on having de fi ned end points, and in the case of animal studies, this has generally been serial ... See full document
15
Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease
... kidney disease. Of these, in 217 patients (47%) an underlying genetic kidney disease was likely, in 184 patients (40%), the respective renal diagnoses for patients and relatives were ... See full document
11
Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney Disorders and European Renal Best Practice
... and kidney disease [13, 14], and with the 35% reduction in decline in creatinine clearance in the study that tested angiotensin-converting enzyme inhibition in patients with type 1 diabetes and ... See full document
12
Incidence and survival of end-stage kidney disease due to polycystic kidney disease in Australia and New Zealand (1963–2014)
... Recent clinical trials in PKD suggest that a lower blood pressure and the use of renin-angiotensin inhibitors re- duces the growth rate of renal cysts in PKD (albeit to a small extent of ~14% over an 8 year period) but ... See full document
12
<p>Regression of Peritubular Capillaries Coincides with Angiogenesis and Renal Cyst Growth in Experimental Polycystic Kidney Disease</p>
... capillaries. 12 A second possibility is that peritubular capillary loss could lead to a vicious cycle of hypoxia, fi brosis and further loss of endothelial cells. 23 From a therapeutic view- point, it would be important ... See full document
12
Chronic asymptomatic pyuria precedes overt urinary tract infection and deterioration of renal function in autosomal dominant polycystic kidney disease
... or kidney volume as an out- come. However, measuring total kidney volume should be considered in the future studies, as this parameter has been used as a surrogate marker for renal function deteri- oration ... See full document
9
A model to predict disease progression in patients with autosomal dominant polycystic kidney disease (ADPKD): the ADPKD Outcomes Model
... including polycystic liver disease or cardiovascular disease, were not modelled due to a lack of published data on the prevalence of ADPKD-related complica- ... See full document
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